Revision coated femoral stem prosthesis - UK MHRA Medical Device Registration

Revision coated femoral stem prosthesis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122995. The device is manufactured by Biomet Orthopaedics from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet UK Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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General Medical Device

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Revision coated femoral stem prosthesis

MHRA Device ID: 122995•Ref: 122995

Device Type

General Medical Device

Devices

Revision coated femoral stem prosthesis

Type

Custom-made - Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

Biomet Orthopaedics

Address

56 East Bell Drive P.O. Box 587

Warsaw, Indiana , United States

Created Date

May 26, 2021

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

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Revision coated femoral stem prosthesis - UK MHRA Medical Device Registration

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Date Registered

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